Variant report

Variant	rs4629479
Chromosome Location	chr4:80595531-80595532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12645453	0.94[ASN][1000 genomes]
rs17447715	0.93[ASN][1000 genomes]
rs4339239	1.00[ASN][1000 genomes]
rs4412018	0.86[ASN][1000 genomes]
rs4536956	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4569784	0.86[ASN][1000 genomes]
rs4594745	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4975103	0.98[ASN][1000 genomes]
rs4975105	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4975106	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4975108	0.96[ASN][1000 genomes]
rs55981032	0.96[ASN][1000 genomes]
rs56204003	0.80[ASN][1000 genomes]
rs62297307	0.98[ASN][1000 genomes]
rs62297310	0.92[ASN][1000 genomes]
rs62297311	0.91[ASN][1000 genomes]
rs6823216	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72649355	0.98[ASN][1000 genomes]
rs7656466	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879506	chr4:80316417-80604625	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1002031	chr4:80459528-80759113	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1005152	chr4:80549659-80814456	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv997478	chr4:80578536-80669871	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1006225	chr4:80578536-80670045	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80594400-80596000	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr4:80594600-80595800	Enhancers	Dnd41	blood
3	chr4:80594600-80596000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:80594600-80596000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:80594800-80596000	Enhancers	Primary B cells from peripheral blood	blood
6	chr4:80594800-80596200	Enhancers	Primary hematopoietic stem cells	blood
7	chr4:80595400-80596000	Enhancers	Primary B cells from cord blood	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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